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Neurological Surgery No Shinkei Geka Volume 20, Issue 11 （November 1992）

Neurological Surgery 脳神経外科 20巻11号（1992年11月発行）

Japanese English

症例

Subfrontal Schwannomaの1例 A Case of Subfrontal Schwannoma 坂東一彦 ^1,2 , 大林正明 ¹ , 深見常晴 ¹ Kazuhiko BANDO ^1,2 , Masaaki OBAYASHI ¹ , Fukami TSUNEHARU ¹ ¹大分中村病院脳神経外科 ²徳島大学脳神経外科 ¹Department of Neurosurgery, Oita Nakamura Hospital キーワード： Subfrontal schwannoma , Intranasal schwannoma , Anterior skull base Keyword: Subfrontal schwannoma , Intranasal schwannoma , Anterior skull base pp.1189-1194

発行日 1992年11月10日 Published Date 1992/11/10

DOI https://doi.org/10.11477/mf.1436900558

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Abstract 文献概要
1ページ目 Look Inside

I．はじめに

　頭蓋内の神経鞘腫の多くは聴神経に発生し，次いで三叉神経にみられるが，前頭蓋底に発生する神経鞘腫，すなわちsubfrontal schwannomaは極めて稀で，現在までに11例^{1,6,8,14,15,20,22,23,25-27）}の報告があるに過ぎない．今回，われわれは鼻腔，篩骨洞から前頭蓋底に至るsubfrontal schwannomaの1例を経験したので報告する．

We encountered a rare case of subfrontal schwannoma. A 55-year-old woman had received resection of a left frontal tumor because of hyposmia, at the age of 28 years. on June 10, 1989, she was admitted with the chief complaint of progressive contraction of visual field. Neu-rologic examination revealed anosmia, impaired vision and concentric contraction of visual field. Fundoscopy showed optic atrophy.

CT examination demonstrated a calcified mass of mixed density which was occupying her nasal cavity, ethmoid sinus and anterior skull base. The lesion was en-hanced with contrast medium. MRI clearly depicted the extension of the lesion and a low signal intensity area in the left frontal lobe as a postoperative scar. Angiography showed hypovascularity.

The tumor was totally removed by bifrontal cra-niotomy on August 22, 1989. Infiltration into the brain or compression of the optic nerve was not detected. The dura on the cranial base side was damaged and lost by infiltration of the tumor, normal olfactory bulb was not able to be identified, and the cribrifrom plate was broken. The anterior skull base was reconstituted bycovering the dttral defect with cadaveric dura and the bony defect with a pericranium.

HE staining showed Antoni A&B types of schwanno-ma. Postoperative course was uneventful. In this case, it is most likely that a remnant of the tumor resected when she was 28 years old had developed subfrontal schwannoma a long time after the operation, although the histological type at that time was unknown. It is also possible that a primary tumor in the nasal cav-ity or paranasal sinus may have extended into the cra-nium. Of 11 reports of subfrontal schwannoma, 2 reports describe extracranial extension to the paranasal sinus.Primary schwannoma in the nasal cavity or paranasal sinus was reported to extend to the anterior skull base in 3 cases, and to the middle cranial fossa in 4 cases of 87 cases reported.

In our case, the possible subfrontal schwannoma is assumed to have originated from 1) the meningeal branch of the trigeminal nerve or the anterior ethmoid nerve, 2) aberration, or 3) the perivascular nerve plexus in the pia mater. However, the definite orgin was not able to be lo-cated owing to the previous operation.